Primary Device ID | 08437006085434 |
NIH Device Record Key | a1c8c128-ba31-4d56-8eec-5a09a0e00d88 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cutter |
Version Model Number | SCI0700 |
Company DUNS | 465890437 |
Company Name | NEOS SURGERY SL |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 0935944726 |
info@neosurgery.com | |
Phone | 0935944726 |
info@neosurgery.com | |
Phone | 0935944726 |
info@neosurgery.com | |
Phone | 0935944726 |
info@neosurgery.com | |
Phone | 0935944726 |
info@neosurgery.com | |
Phone | 0935944726 |
info@neosurgery.com | |
Phone | 0935944726 |
info@neosurgery.com | |
Phone | 0935944726 |
info@neosurgery.com | |
Phone | 0935944726 |
info@neosurgery.com | |
Phone | 0935944726 |
info@neosurgery.com | |
Phone | 0935944726 |
info@neosurgery.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08437006085434 [Primary] |
LXH | Orthopedic Manual Surgical Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08437006085434]
Moist Heat or Steam Sterilization
[08437006085434]
Moist Heat or Steam Sterilization
[08437006085434]
Moist Heat or Steam Sterilization
[08437006085434]
Moist Heat or Steam Sterilization
[08437006085434]
Moist Heat or Steam Sterilization
[08437006085434]
Moist Heat or Steam Sterilization
[08437006085434]
Moist Heat or Steam Sterilization
[08437006085434]
Moist Heat or Steam Sterilization
[08437006085434]
Moist Heat or Steam Sterilization
[08437006085434]
Moist Heat or Steam Sterilization
[08437006085434]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-09-12 |
Device Publish Date | 2024-09-04 |
08437006085182 - Depth Gauge | 2024-09-12 DEPTH GAUGE |
08437006085212 - Retractor | 2024-09-12 |
08437006085434 - Cutter | 2024-09-12 |
08437006085434 - Cutter | 2024-09-12 |
28437006085452 - STERN FIX | 2024-09-12 STERN FIX Sternal Stabilization System, Size 2 |
28437006085469 - STERN FIX | 2024-09-12 STERN FIX Sternal Stabilization System- size 3 |
08437006085472 - STERN FIX | 2024-09-12 STERN FIX Sternal Stabilization System-Size 4 |
28437006085483 - STERN FIX | 2024-09-12 STERN FIX Sternal Stabilization System- Size 5 |
08437006085496 - Forceps | 2024-09-12 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CUTTER 97820387 not registered Live/Pending |
United Industries Corporation 2023-03-02 |
CUTTER 97564943 not registered Live/Pending |
Global Tobacco, LLC 2022-08-25 |
CUTTER 97305519 not registered Live/Pending |
Linzer Products Corp. 2022-03-10 |
CUTTER 90532872 not registered Live/Pending |
United Industries Corporation 2021-02-17 |
CUTTER 90502340 not registered Live/Pending |
United Industries Corporation 2021-02-01 |
CUTTER 90502311 not registered Live/Pending |
United Industries Corporation 2021-02-01 |
CUTTER 90212930 not registered Live/Pending |
United Industries Corporation 2020-09-26 |
CUTTER 88886942 not registered Live/Pending |
United Industries Corporation 2020-04-24 |
CUTTER 87226981 not registered Dead/Abandoned |
United Industries Corporation 2016-11-04 |
CUTTER 86501045 5453846 Live/Registered |
United Industries Corporation 2015-01-12 |
CUTTER 86306302 not registered Dead/Abandoned |
United Industries Corporation 2014-06-11 |
CUTTER 86088498 4521956 Live/Registered |
United Industries Corporation 2013-10-10 |